001     301745
005     20250819093625.0
024 7 _ |a 10.1093/nar/gkaf435
|2 doi
024 7 _ |a pmid:40444638
|2 pmid
024 7 _ |a pmc:PMC12123414
|2 pmc
024 7 _ |a 0305-1048
|2 ISSN
024 7 _ |a 0261-3166
|2 ISSN
024 7 _ |a 1362-4954
|2 ISSN
024 7 _ |a 1362-4962
|2 ISSN
024 7 _ |a 1746-8272
|2 ISSN
024 7 _ |a altmetric:177660179
|2 altmetric
037 _ _ |a DKFZ-2025-01129
041 _ _ |a English
082 _ _ |a 570
100 1 _ |a Gehrs, Stephanie
|0 P:(DE-He78)6c7c0079533d7a9cda3bb9f463e22ccb
|b 0
|e First author
|u dkfz
245 _ _ |a DNMT3A-dependent DNA methylation shapes the endothelial enhancer landscape.
260 _ _ |a Oxford
|c 2025
|b Oxford Univ. Press
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1755588960_6400
|2 PUB:(DE-HGF)
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a Journal Article
|0 0
|2 EndNote
500 _ _ |a #EA:A190#LA:A190#LA:B370# / geteilte Letztautorenschaft aus unterschiedlichen Kostenstellen
520 _ _ |a DNA methylation plays a fundamental role in regulating transcription during development and differentiation. However, its functional role in the regulation of endothelial cell (EC) transcription during state transition, meaning the switch from an angiogenic to a quiescent cell state, has not been systematically studied. Here, we report the longitudinal changes of the DNA methylome over the lifetime of the murine pulmonary vasculature. We identified prominent alterations in hyper- and hypomethylation during the transition from angiogenic to quiescent ECs. Once a quiescent state was established, DNA methylation marks remained stable throughout EC aging. These longitudinal differentially methylated regions correlated with endothelial gene expression and highlighted the recruitment of de novo DNA methyltransferase 3a (DNMT3A), evidenced by its motif enrichment at transcriptional start sites of genes with methylation-dependent expression patterns. Loss-of-function studies in mice revealed that the absence of DNMT3A-dependent DNA methylation led to the loss of active enhancers, resulting in mild transcriptional changes, likely due to loss of active enhancer integrity. These results underline the importance of DNA methylation as a key epigenetic mechanism of EC function during state transition. Furthermore, we show that DNMT3A-dependent DNA methylation appears to be involved in establishing the histone landscape required for accurate transcriptome regulation.
536 _ _ |a 311 - Zellbiologie und Tumorbiologie (POF4-311)
|0 G:(DE-HGF)POF4-311
|c POF4-311
|f POF IV
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed, , Journals: inrepo02.dkfz.de
650 _ 7 |a DNA Methyltransferase 3A
|0 EC 2.1.1.37
|2 NLM Chemicals
650 _ 7 |a DNA (Cytosine-5-)-Methyltransferases
|0 EC 2.1.1.37
|2 NLM Chemicals
650 _ 7 |a Dnmt3a protein, mouse
|2 NLM Chemicals
650 _ 7 |a DNMT3A protein, human
|2 NLM Chemicals
650 _ 2 |a DNA Methylation
|2 MeSH
650 _ 2 |a DNA Methyltransferase 3A
|2 MeSH
650 _ 2 |a Animals
|2 MeSH
650 _ 2 |a DNA (Cytosine-5-)-Methyltransferases: genetics
|2 MeSH
650 _ 2 |a DNA (Cytosine-5-)-Methyltransferases: metabolism
|2 MeSH
650 _ 2 |a Mice
|2 MeSH
650 _ 2 |a Endothelial Cells: metabolism
|2 MeSH
650 _ 2 |a Enhancer Elements, Genetic
|2 MeSH
650 _ 2 |a Epigenesis, Genetic
|2 MeSH
650 _ 2 |a Neovascularization, Physiologic: genetics
|2 MeSH
650 _ 2 |a Gene Expression Regulation
|2 MeSH
650 _ 2 |a Humans
|2 MeSH
700 1 _ |a Gu, Zuguang
|b 1
700 1 _ |a Hey, Joschka
|0 P:(DE-He78)198a73f54b40192a2fdc2bf53ba7ca27
|b 2
700 1 _ |a Weichenhan, Dieter
|0 P:(DE-He78)ff4024f7bc236e7897d9c18ee19c451f
|b 3
|u dkfz
700 1 _ |a Buckwalter, Niklas
|0 P:(DE-He78)bb8874c831d15fe8fcb9946f98723770
|b 4
|u dkfz
700 1 _ |a Jakab, Moritz Viktor
|0 P:(DE-He78)e17ab05b2c7ece91a9ce3e8355fd3825
|b 5
700 1 _ |a Hotz-Wagenblatt, Agnes
|0 P:(DE-He78)2f34b89d62d5e5c651aa1e683844b092
|b 6
700 1 _ |a Breuer, Kersten
|0 P:(DE-He78)75efcd61c13c2fbe457cdf3454ef486c
|b 7
700 1 _ |a Prada, Maria Llamazares
|0 P:(DE-HGF)0
|b 8
700 1 _ |a Hübschmann, Daniel
|0 P:(DE-He78)a5218e4871866cd5ab2312e594ca403d
|b 9
|u dkfz
700 1 _ |a Schlereth, Katharina
|0 P:(DE-He78)e674edaa6403c4ef34b2fae4649e654f
|b 10
700 1 _ |a Plass, Christoph
|0 P:(DE-He78)4301875630bc997edf491c694ae1f8a9
|b 11
|e Last author
|u dkfz
700 1 _ |a Augustin, Hellmut
|0 P:(DE-He78)2e92d0ae281932fc7347d819fec36b0b
|b 12
|e Last author
|u dkfz
773 _ _ |a 10.1093/nar/gkaf435
|g Vol. 53, no. 10, p. gkaf435
|0 PERI:(DE-600)1472175-2
|n 10
|p gkaf435
|t Nucleic acids research
|v 53
|y 2025
|x 0305-1048
909 C O |p VDB
|o oai:inrepo02.dkfz.de:301745
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 0
|6 P:(DE-He78)6c7c0079533d7a9cda3bb9f463e22ccb
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 2
|6 P:(DE-He78)198a73f54b40192a2fdc2bf53ba7ca27
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 3
|6 P:(DE-He78)ff4024f7bc236e7897d9c18ee19c451f
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 4
|6 P:(DE-He78)bb8874c831d15fe8fcb9946f98723770
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 5
|6 P:(DE-He78)e17ab05b2c7ece91a9ce3e8355fd3825
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 6
|6 P:(DE-He78)2f34b89d62d5e5c651aa1e683844b092
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 7
|6 P:(DE-He78)75efcd61c13c2fbe457cdf3454ef486c
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 8
|6 P:(DE-HGF)0
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 9
|6 P:(DE-He78)a5218e4871866cd5ab2312e594ca403d
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 10
|6 P:(DE-He78)e674edaa6403c4ef34b2fae4649e654f
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 11
|6 P:(DE-He78)4301875630bc997edf491c694ae1f8a9
910 1 _ |a Deutsches Krebsforschungszentrum
|0 I:(DE-588b)2036810-0
|k DKFZ
|b 12
|6 P:(DE-He78)2e92d0ae281932fc7347d819fec36b0b
913 1 _ |a DE-HGF
|b Gesundheit
|l Krebsforschung
|1 G:(DE-HGF)POF4-310
|0 G:(DE-HGF)POF4-311
|3 G:(DE-HGF)POF4
|2 G:(DE-HGF)POF4-300
|4 G:(DE-HGF)POF
|v Zellbiologie und Tumorbiologie
|x 0
914 1 _ |y 2025
915 _ _ |a Nationallizenz
|0 StatID:(DE-HGF)0420
|2 StatID
|d 2024-12-10
|w ger
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
|d 2024-12-10
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
|d 2024-12-10
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0501
|2 StatID
|b DOAJ Seal
|d 2024-04-03T10:37:02Z
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0500
|2 StatID
|b DOAJ
|d 2024-04-03T10:37:02Z
915 _ _ |a Peer Review
|0 StatID:(DE-HGF)0030
|2 StatID
|b DOAJ : Anonymous peer review
|d 2024-04-03T10:37:02Z
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Clarivate Analytics Master Journal List
|d 2024-12-10
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1050
|2 StatID
|b BIOSIS Previews
|d 2024-12-10
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0160
|2 StatID
|b Essential Science Indicators
|d 2024-12-10
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1030
|2 StatID
|b Current Contents - Life Sciences
|d 2024-12-10
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1190
|2 StatID
|b Biological Abstracts
|d 2024-12-10
915 _ _ |a WoS
|0 StatID:(DE-HGF)0113
|2 StatID
|b Science Citation Index Expanded
|d 2024-12-10
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
|d 2024-12-10
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
|b NUCLEIC ACIDS RES : 2022
|d 2024-12-10
915 _ _ |a IF >= 10
|0 StatID:(DE-HGF)9910
|2 StatID
|b NUCLEIC ACIDS RES : 2022
|d 2024-12-10
915 _ _ |a Article Processing Charges
|0 StatID:(DE-HGF)0561
|2 StatID
|d 2024-12-10
915 _ _ |a Fees
|0 StatID:(DE-HGF)0700
|2 StatID
|d 2024-12-10
920 2 _ |0 I:(DE-He78)A190-20160331
|k A190
|l A190 Vaskuläre Onkologie und Metastasierung
|x 0
920 2 _ |0 I:(DE-He78)B370-20160331
|k B370
|l Epigenomik
|x 1
920 1 _ |0 I:(DE-He78)A190-20160331
|k A190
|l A190 Vaskuläre Onkologie und Metastasierung
|x 0
920 1 _ |0 I:(DE-He78)B370-20160331
|k B370
|l Epigenomik
|x 1
920 1 _ |0 I:(DE-He78)W015-20160331
|k W015
|l Innovations- und Service-Unit für Bioinformatik und Präzisionsmedizin
|x 2
920 1 _ |0 I:(DE-He78)HD01-20160331
|k HD01
|l DKTK HD zentral
|x 3
920 1 _ |0 I:(DE-He78)W610-20160331
|k W610
|l Core Facility Omics IT
|x 4
920 0 _ |0 I:(DE-He78)A190-20160331
|k A190
|l A190 Vaskuläre Onkologie und Metastasierung
|x 0
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a I:(DE-He78)A190-20160331
980 _ _ |a I:(DE-He78)B370-20160331
980 _ _ |a I:(DE-He78)W015-20160331
980 _ _ |a I:(DE-He78)HD01-20160331
980 _ _ |a I:(DE-He78)W610-20160331
980 _ _ |a UNRESTRICTED


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21